Pyrylium-mediated transformations of natural products. Part 9. The effect of temperature and ionic strength on the mechanism and rate of reactions of pyridinium ions in aqueous solution

In this work, the adsorption of crystal violet dye from aqueous solution on charcoal and rice husk has been investigated, where the impact of variable factors (contact time; the dosage of adsorbent, pH, temperature, and ionic strength) have been studied. It has been found that charcoal and rice husk have an appropriate adsorption limit with regards to the expulsion of crystal violet dye from fluid arrangements. The harmony adsorption is for all intents and purposes accomplished in 45 min for charcoal and 60 min for rice husk. The amount of crystal violet dye adsorbed (0.4 g of charcoal and 0.5 g of rice husk) increased with an increasing pH and the value of 11 is the best. The effect of temperature on the adsorption process was studied at the range (298-323) K. The test comes about were broken down by utilizing Freundlich and Tempkin isotherm models, where the Freundlich and Tempkin factors were determined, and it has been found that the adsorption isotherm obey the Freundlich isotherm. The effect of ionic strength on the adsorption process was studied also via sodium chloride electrolyte solution; the results have been revaled that the sodium ion has a positive impact on the adsorption process. The thermodynamic parameters are shown estimated as ∆H values were 2.8012 kJ mol-1 and 5.8252 kJ mol-1 for charcoal and rice husk, respectively; this behavior referred to endothermic adsorption.

Download Full-text

ChemInform Abstract: PYRYLIUM-MEDIATED TRANSFORMATIONS OF NATURAL PRODUCTS. PART 7. DISPLACEMENT OF THE N-SUBSTITUENTS OF PYRIDINIUM IONS IN AQUEOUS SOLUTION: REPLACEMENT OF THE Ω-AMINO GROUP OF LYSINE, AND OF THE TERMINAL AMINO GROUP OF GLYCYLGLYCINE

Chemischer Informationsdienst ◽

10.1002/chin.198434195 ◽

1984 ◽

Vol 15 (34) ◽

Author(s):

A. R. KATRITZKY ◽

Y.-K. YANG

Keyword(s):

Aqueous Solution ◽

Natural Products ◽

Amino Group ◽

Terminal Amino ◽

Pyridinium Ions

Download Full-text

Temperature Effect on the Two-Dimensional Phase Transition Kinetics of Adenine Adsorbed at the Hg Electrode/Aqueous Solution Interface

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc20031407 ◽

2003 ◽

Vol 68 (8) ◽

pp. 1407-1419 ◽

Cited By ~ 3

Author(s):

Claudio Fontanesi ◽

Roberto Andreoli ◽

Luca Benedetti ◽

Roberto Giovanardi ◽

Paolo Ferrarini

Keyword(s):

Phase Transition ◽

Aqueous Solution ◽

Phase Change ◽

Temperature Effect ◽

Transition Rate ◽

Effect Of Temperature ◽

Two Dimensional ◽

Solution Interface ◽

Phase Transition Kinetics ◽

Kinetics Of

The kinetics of the liquid-like → solid-like 2D phase transition of adenine adsorbed at the Hg/aqueous solution interface is studied. Attention is focused on the effect of temperature on the rate of phase change; an increase in temperature is found to cause a decrease of transition rate.

Download Full-text

Meso tetrakis ortho-, meta-, and para-N-alkylpyridiniopor-phyrins: kinetics of copper(II) and zinc(II) incorporation and zinc porphyrin demetalation

Journal of Porphyrins and Phthalocyanines ◽

10.1142/s1088424603000197 ◽

2003 ◽

Vol 07 (03) ◽

pp. 139-146 ◽

Cited By ~ 6

Author(s):

Peter Hambright ◽

Ines Batinić-Haberle ◽

Ivan Spasojević

Keyword(s):

Aqueous Solution ◽

Ionic Strength ◽

Effective Charge ◽

Methyl Ethyl ◽

Ionic Strength Dependence ◽

Zinc Porphyrin ◽

Cationic Porphyrin ◽

Strength Dependence ◽

Acid Catalyzed ◽

Kinetics Of

The relative reactivities of the tetrakis( N -alkylpyridinium- X - yl )-porphyrins where X = 4 (alkyl = methyl, ethyl, n -propyl) , X = 3 (methyl) , and X = 2 (methyl, ethyl, n -propyl, n -butyl, n -hexyl, n -octyl) were studied in aqueous solution. From the ionic strength dependence of the metalation rate constants, the effective charge of a particular cationic porphyrin was usually larger when copper(II) rather than zinc(II) was the reactant. The kinetics of ZnOH + incorporation and the acid catalyzed removal of zinc from the porphyrins in 1.0 M HCl were also studied. In general, the more basic 4- (para-) and 3- (meta-) isomers were the most reactive, followed by the less basic 2- (ortho-) methyl to n -butyl derivatives, with the lipophilic ortho n -hexyl and n -octyl porphyrins the least reactive.

Download Full-text

Determination of the complexation properties of a crosslinked poly(acrylic acid) gel with copper(II), nickel(II), and lead(II) in dilute aqueous solution

Canadian Journal of Chemistry ◽

10.1139/v01-059 ◽

2001 ◽

Vol 79 (4) ◽

pp. 370-376 ◽

Cited By ~ 5

Author(s):

Catherine Morlay ◽

Yolande Mouginot ◽

Monique Cromer ◽

Olivier Vittori

Keyword(s):

Aqueous Solution ◽

Ionic Strength ◽

Acrylic Acid ◽

Metal Ion ◽

Conditional Stability ◽

Binding Properties ◽

Complex Species ◽

Complexing Capacity ◽

Dilute Aqueous Solution ◽

Poly Acrylic Acid

The possible removal of copper(II), nickel(II), or lead(II) by an insoluble crosslinked poly(acrylic acid) was investigated in dilute aqueous solution. The binding properties of the polymer were examined at pH = 6.0 or 4.0 with an ionic strength of the medium µ = 0.1 or 1.0 M (NaNO3) using differential pulse polarography as an investigation means. The highest complexing capacity of the polyacid was obtained with lead(II) at pH = 6.0 with µ = 0.1 M, 4.8 mmol Pb(II)/g polymer. The conditional stability constants of the complex species formed were determined using the method proposed by Ruzic assuming that only the 1:1 complex species was formed; for lead(II) at pH = 6.0 and µ = 0.1 M, log K' = 5.3 ± 0.2. It appeared that the binding properties of the polymer increased, depending on the metal ion, in the following order: Ni(II) < Cu(II) < Pb(II). The complexing capacity and log K' values decreased with the pH or with an increase of the ionic strength. These results were in agreement with the conclusions of our previous studies of the hydrosoluble linear analogues. Finally, with the insoluble polymer, the log K' values were comparable to those previously obtained with the linear analogue whereas the complexing capacity values expressed in mmol g-1 were slightly lower.Key words: insoluble crosslinked poly(acrylic acid), copper(II), nickel(II), and lead(II) complexation.

Download Full-text

Inerte Amminkomplexe als mehrwertige Kationsäuren in wäßriger Lösung / Inert Ammine Complexes as Multivalent Cationic Acids in Aqueous Solution

Zeitschrift für Naturforschung B ◽

10.1515/znb-1980-0907 ◽

1980 ◽

Vol 35 (9) ◽

pp. 1096-1103 ◽

Cited By ~ 3

Author(s):

Matthias Kretschmer ◽

Lutwin Labouvie ◽

Karl-W. Quirin ◽

Helmut Wiehn ◽

Ludwig Heck

Keyword(s):

Aqueous Solution ◽

Ionic Strength ◽

Spectrophotometric Method ◽

Complex Cation ◽

Aqua Ligand ◽

Second Step ◽

Acidity Constants ◽

Ammine Complexes ◽

Temperature Variations ◽

Enthalpy Changes

Acidity constants of ammine complexes of tetravalent platinum in aqueous solutions have been determined by a spectrophotometric method at very low ionic strengths and extrapolated to zero ionic strength. Temperature variations of pK-values (25 °C and 50 °C) yield thermodynamic parameters for two successive deprotonation steps of hexaammineplatinum(IV), pentaamminechloroplatinum(IV), and tris(ethylenediamine)pla- tinum(IV) complexes and for the deprotonation of pentaammineaquacobalt(III) ion.The enthalpy changes for the first and second steps are similar and range from 50 to 75 kJ/mole while for the aqua ligand of Co(III) 33 kJ/mole are found. The very large difference in the entropy changes (about 70 to 80 J/K mole for the first step and -10 to + 20 J/K mole for the second step) is interpreted by a model of solvation change. The primary hydration sphere of strongly oriented and immobilized water dipoles around the highly charged complex cation is transformed to a hydrogen-bonded solvation sheath when the electric field of the complex is weakened upon release of the first proton.

Download Full-text